DMAP Catalyzed Domino Rauhut–Currier Cyclization Reaction between Alkylidene Pyrazolones and Nitro-olefins: Access to Tetrahydropyrano[2,3-<i>c</i>]pyrazoles
Nimisha Bania, Buddhadeb Mondal, Sounak Ghosh, Subhas Chandra Pan
Abstract
Herein, we employ unsaturated pyrazolones in the Rauhut–Currier reaction for the first time. A domino Rauhut–Currier cyclization reaction has been developed between unsaturated pyrazolones and nitro-olefins. The trisubstituted tetrahydropyrano[2,3-c]pyrazoles were obtained in moderate to high yields with excellent diastereoselectivities. A few applications including a synthesis of disubstituted tetrahydropyrano[2,3-c]pyrazole have been demonstrated. A preliminary catalytic asymmetric version of this process was also studied with chiral DMAP catalysts.
Topics & Concepts
PyrazolonesDominoChemistryNitroCatalysisPyrazoleCascade reactionMedicinal chemistryOrganic chemistryAlkylMulticomponent Synthesis of HeterocyclesSynthesis of Indole DerivativesSynthesis of heterocyclic compounds